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Journal of Molecular and Cellular Cardiology|July 28, 2004
Arginase pathway in human endothelial cells in pathophysiological conditionsTiziana Bachetti, Laura Comini, Gloria Francolini, et al.
Gene|March 5, 2025
A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysisMuhammad Abrar Yousaf, Arianna Scartezzini, Chiara Colombo, et al.
Molecular Therapy. Nucleic Acids|September 27, 2024
Identification of a histone deacetylase inhibitor as a therapeutic candidate for congenital central hypoventilation syndromeChiara Africano, Tiziana Bachetti, Paolo Uva, et al.
Genes|December 16, 2020
Alexander Disease Modeling in Zebrafish: An In Vivo System Suitable to Perform Drug ScreeningSimona Candiani, Silvia Carestiato, Andreas F Mack, et al.
American Journal of Medical Genetics|October 31, 2002
Mutational analysis of the RNX gene in congenital central hypoventilation syndromeIvana Matera, Tiziana Bachetti, Roberta Cinti, et al.
Annals of the Rheumatic Diseases|November 3, 2012
Autophagy contributes to inflammation in patients with TNFR-associated periodic syndrome (TRAPS)Tiziana Bachetti, Sabrina Chiesa, Patrizio Castagnola, et al.
The American Journal of Pathology|August 29, 2006
A model of insulin resistance and nonalcoholic steatohepatitis in rats: role of peroxisome proliferator-activated receptor-alpha and n-3 polyunsaturated fatty acid treatment on liver injuryGianluca Svegliati-Baroni, Cinzia Candelaresi, Stefania Saccomanno, et al.
European Journal of Internal Medicine|July 2, 2025
Modulation of hypoxia-sensitive non-coding RNAs following continuous positive airway pressure therapy in obstructive sleep apnea in peripheral bloodFrancesco Fanfulla, Veronica Barbi, Tiziana Bachetti, et al.
Annals of Human Genetics|October 16, 2010
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activitiesTiziana Bachetti, Eleonora Di Zanni, Francesca Lantieri, et al.
European Journal of Human Genetics : EJHG|May 17, 2007
Transcriptional regulation of TLX2 and impaired intestinal innervation: possible role of the PHOX2A and PHOX2B genesSilvia Borghini, Marco Di Duca, Giuseppe Santamaria, et al.
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